Same here.
The thread was started by Laura and Linda back in '05, I think in May. Anyway, it was a thread where survivors checked in. Luckily, I frequented the Community thread a lot in those long ago days and found it immediately. I think I might be on the first page of the original thread. Right away we had another of our original members going through the diagnosis stage.
Since then we have welcomed survivors, relatives and friends of survivors, and other good friends.
We tend to get off topic a lot but that can be a good thing.
I have been fortunate enough to meet Laura and one of her daughters, Ann and her lovely sisters, Maureen and her fantastic family, and Alison who we have not heard from in awhile. I am hoping to meet more in the future.
I too was diagnosed in 2004 at age 50, had a modified radical since I had multicentric in situ cancer (DCIS on steriods) with just a minimal area of invasive cancer, thank goodness. I had 16 clean nodes removed, so no chemo or radiation was deemed necesary.
I did have those dreaded drains in for what seemed to be an eternity, those were the worst, and the surgeon said no showers so my DH helped me bathe too for about a month until the last drain was pulled.
And recovering from the node dissection has its own lovely aspects.
Also, my blood pressure and thyroid function decided to flare up at the same time. I think I aged a lot in 2004.
But, so far so good, in fact I got brave and did reconstruction in 2006 after agonizing over it and driving everyone here insane no doubt mulling it over, checking out plastic surgeons, getting a second and a third opinion.
I ended up finding the right doc for me, and had a free tram flap. More surgery, more drains, but it was a big improvement for me over dealing with a large, heavy prothesis in our south Louisiana climate.
Best move I made in the whole saga.
I will also have to credit the ladies here for being so supportive back in 2005 when our family and friends living in New Orleans went through Katrina and lived with us for awhile.
It helped to come here to the thread (when I had my alloted time on the computer which was our main avenue of communication for awhile) and connect with my sistas here when I had all those extra people and one extra doggie living in my house. We had issues even here 70 mile northwest of New Orleans since so many people evacuated, getting gas and food, and the difficulty of just getting anywhere with the roads clogged with the instant increase in our population persists today.
I felt good enough about myself to venture back into the work world in a quasi part time status in September 2007 (I sort of got recruited at a non-profit by my mom's late friend whose daughter is my boss and was looking for angel to help her). Back in the day, I worked for a big company in New Orleans for many years but "retired" at age 45 in 1998 when we moved here. Being employed again has turned out to be a blessing as I feel sharper mentally (accounting tends to make you analyze everything you do

) and we certainly need the extra coins with two in college, and one in the bull-pen (7th grade).
I feel blessed to have all my friends here. I have a lot of support in my life from DH, my mom, my sister, and my brother Tom in NYC, not to mention my friends and family in New Orleans, but there is nothing like talking to someone who has walked in your shoes so to speak.
I was even able to support my mom when she was diagnosed with extensive DCIS September 2008. She lavishes me with appreciation (it is almost embarrassing), and man does it feel good to have been able to help her through her surgery and reconstruction (yes a 78 year old with an expander).
Now I mainly worry about my daughters might face in the future, one is 18, the other 13, and my sister who is 51, and has already had 3 biopsies.
Hoping for a cure, or at least better, earlier detection. Less drastic surgery would be nice too.
But hooray for survivors, hooray for Laura and LInda for starting this thread, and hooray for all you sistas.
As WDW lovers AND survivors, one day we all need to try and meet for the Orlando RFTC. I have been two years running now, once with mom, last year with my DH. We met up with sisters from this thread both times.
WDW in October is amazing, and now that the RFTC is in October you get to do the Food and wine festival too. It is an embarrassment of riches. When I get frustrated with the accounting gig, I remember how much I treasure those trips, and I keep my nose to the grindstone.
Going to visit Micky is expensive. It is a sin that insurance doesn't cover 80% of the cost.
Maybe we can get that coverage into the next stimulus package.
OK that is my "story."
I bet others will introduce themselves as well.
Again, welcome to the GAGWTA! thread!